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Target5-hydroxytryptamine receptor 5A
LigandBDBM135787
Substrate/Competitorn/a
Meas. Tech.Binding Inhibition Assay
pH7.5±n/a
Temperature298.15±n/a K
Ki 7.1±n/a nM
Commentsextracted
Citation Kinoyama, IMiyazaki, TKoganemaru, YWashio, THamaguchi, W Nitrogenous-ring acylguanidine derivative US Patent US8853242 Publication Date 10/7/2014
More Info.:Get all data from this article,  Assay Method
 
5-hydroxytryptamine receptor 5A
Name:5-hydroxytryptamine receptor 5A
Synonyms:5-HT-5 | 5-HT-5A | 5-hydroxytryptamine receptor 5 (5-HT5) | 5-hydroxytryptamine receptor 5A (5-HT5A) | 5HT5A_HUMAN | HTR5A | Serotonin (5-HT) receptor | Serotonin receptor 5A
Type:Enzyme
Mol. Mass.:40266.25
Organism:Homo sapiens (Human)
Description:P47898
Residue:357
Sequence:
MDLPVNLTSFSLSTPSPLETNHSLGKDDLRPSSPLLSVFGVLILTLLGFLVAATFAWNLL
VLATILRVRTFHRVPHNLVASMAVSDVLVAALVMPLSLVHELSGRRWQLGRRLCQLWIAC
DVLCCTASIWNVTAIALDRYWSITRHMEYTLRTRKCVSNVMIALTWALSAVISLAPLLFG
WGETYSEGSEECQVSREPSYAVFSTVGAFYLPLCVVLFVYWKIYKAAKFRVGSRKTNSVS
PISEAVEVKDSAKQPQMVFTVRHATVTFQPEGDTWREQKEQRAALMVGILIGVFVLCWIP
FFLTELISPLCSCDIPAIWKSIFLWLGYSNSFFNPLIYTAFNKNYNSAFKNFFSRQH
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  Blast E-value cutoff:
BDBM135787
n/a
NameBDBM135787
Synonyms:US8853242, 159
TypeSmall organic molecule
Emp. Form.C18H14F2N4O2
Mol. Mass.356.3262
SMILESCOc1cccc(F)c1-c1ncc(F)c2ccc(cc12)C(=O)N=C(N)N |(-5.08,-2.13,;-5.85,-.8,;-5.08,.53,;-5.78,2,;-5,3.33,;-3.47,3.33,;-2.69,2,;-1.15,2,;-3.47,.67,;-2.69,-.67,;-3.47,-2,;-2.69,-3.33,;-1.15,-3.33,;-.38,-4.67,;-.38,-2,;1.15,-2,;1.92,-.67,;1.15,.67,;-.38,.67,;-1.15,-.67,;1.92,2,;1.15,3.33,;3.47,2,;4.23,3.33,;5.78,3.33,;3.47,4.67,)|
Structure
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